TY - JOUR
T1 - Clinical experience with intravenous zoledronic acid in the treatment of male osteoporosis
T2 - Evidence and opinions
AU - Ruza, Ieva
AU - Mirfakhraee, Sasan
AU - Orwoll, Eric
AU - Gruntmanis, Ugis
N1 - I.Ružas afiliācijas ir atšķirīgas Scopus datubāzē un publikācijas PDF variantā. Šajā aprakstā ir norādītas afiliācijas no publikācijas PDF oriģināla.
Funding Information:
Ieva Ruza and Sasan Mirfakhraee declare that they have no conflict of interest. Ugis Gruntmanis has received research funding from Novartis, Procter&Gamble, GSK and Amgen. Eric Orwoll has received funding from Amgen, Merck and Lilly and is on the advisory boards of Merck, Lilly, Amgen and Wright Medical Tech.
PY - 2013/8
Y1 - 2013/8
N2 - Osteoporosis frequently remains underrecognized and undertreated in men. Most osteoporosis-related fractures could be prevented if men at risk would be diagnosed, treated, and remained compliant with therapy. Bisphosphonates, the mainstay of osteoporosis treatment, are potent antiresorptive agents that inhibit osteoclast activity, suppress in vivo markers of bone turnover, increase bone mineral density, decrease fractures, and likely improve survival in men with osteoporosis. The focus of the article is on intravenous zoledronic acid, which may be a preferable alternative to oral bisphosphonate therapy in patients with cognitive dysfunction, the inability to sit upright, polypharmacy, significant gastrointestinal pathology or suspected medication noncompliance. Zoledronic acid is approved in the United States (US) and European Union (EU) as an annual 5 mg intravenous infusion to treat osteoporosis in men. The zoledronic acid 4 mg intravenous dose has been studied in the prevention of bone loss associated with androgen deprivation therapy. This article reviews the evidence for zoledronic acid, currently the most potent bisphosphonate available for clinical use, and its therapeutic effects in the treatment of men with osteoporosis.
AB - Osteoporosis frequently remains underrecognized and undertreated in men. Most osteoporosis-related fractures could be prevented if men at risk would be diagnosed, treated, and remained compliant with therapy. Bisphosphonates, the mainstay of osteoporosis treatment, are potent antiresorptive agents that inhibit osteoclast activity, suppress in vivo markers of bone turnover, increase bone mineral density, decrease fractures, and likely improve survival in men with osteoporosis. The focus of the article is on intravenous zoledronic acid, which may be a preferable alternative to oral bisphosphonate therapy in patients with cognitive dysfunction, the inability to sit upright, polypharmacy, significant gastrointestinal pathology or suspected medication noncompliance. Zoledronic acid is approved in the United States (US) and European Union (EU) as an annual 5 mg intravenous infusion to treat osteoporosis in men. The zoledronic acid 4 mg intravenous dose has been studied in the prevention of bone loss associated with androgen deprivation therapy. This article reviews the evidence for zoledronic acid, currently the most potent bisphosphonate available for clinical use, and its therapeutic effects in the treatment of men with osteoporosis.
KW - bisphosphonates
KW - bone mineral density
KW - fracture
KW - men
KW - osteoporosis
KW - zoledronic acid
UR - http://www.scopus.com/inward/record.url?scp=84887426739&partnerID=8YFLogxK
U2 - 10.1177/1759720X13485829
DO - 10.1177/1759720X13485829
M3 - Article
AN - SCOPUS:84887426739
SN - 1759-720X
VL - 5
SP - 182
EP - 198
JO - Therapeutic Advances in Musculoskeletal Disease
JF - Therapeutic Advances in Musculoskeletal Disease
IS - 4
ER -